Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5218702 | Tetrahedron | 2012 | 8 Pages |
Epidemiological studies indicate that flavonoid intake is inversely associated with the risk of coronary heart disease, yet the mechanisms responsible for their bioactivity are still a matter of debate. Based on the rapid and extensive metabolism of most flavonoids, their health effects most likely result from the biological activity of their metabolites. However, a lack of commercially available compounds/standards has prevented the study of metabolite bioactivity and resulted in a focus on non-physiologically relevant precursor/parent structures. This paper details the synthesis of a series of phenolic glucuronide 1a-e and sulfate 2a-e derivates as candidate metabolites for use as reference compounds in metabolic profiling studies and for the exploration of flavonoid bioactivity.
Graphical AbstractDownload full-size imageTwo sets of candidate metabolites of dietary flavonoids: phenolic glucuronides and sulfates have been synthesised.